Search research articles
Contact Us
Filters
Showing results (271-280 of 582) with videos related to
Page
of 59
Sort By:
Diabetes
|
May 30, 2006
HLA genotyping supports a nonautoimmune etiology in patients diagnosed with diabetes under the age of 6 months
Emma L Edghill, Rachel J Dix, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 29, 2020
Heterozygous Insulin Receptor <i>(INSR)</i> Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series
Aashish Sethi, Nicola Foulds, Sarah Ehtisham, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
January 8, 2015
Complex equilibria, speciation, and heteroprotein coacervation of lactoferrin and β-lactoglobulin
Sean E Flanagan, Alexander J Malanowski, Ebru Kizilay, et al.
BMC Health Services Research
|
July 19, 2023
Rapid implementation of Veterans Health Administration telehealth creative arts therapies: survey evaluation of adoption and adaptation
Kristin M Story, Mindy E Flanagan, Sheri L Robb, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
January 18, 2003
The influence of insulin on circulating ghrelin
Daniel E Flanagan, Mark L Evans, Teresa P Monsod, et al.
Journal of the American Academy of Dermatology
|
January 9, 2022
Use of virtual reality during scalp injections: A randomized interventional crossover study
James T Pathoulas, Kelly E Flanagan, Chloe J Walker, et al.
Pediatric Diabetes
|
June 4, 2021
Identification of GCK-maturity-onset diabetes of the young in cases of neonatal hyperglycemia: A case series and review of clinical features
Alice E Hughes, Elisa De Franco, Evgenia Globa, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 20, 2014
Congenital hyperinsulinism in a newborn with a novel homozygous mutation (p.Q392H) in the ABCC8 gene
Deniz Anuk Ince, Nursel Muratoglu Sahin, Ayse Ecevit, et al.
JDR Clinical and Translational Research
|
December 1, 2025
Indigenous Australians' Oral Health Care Experiences: Recommendations for Culturally Safe Dental Care
R Aiyar, S Nath, J Hedges, et al.
Pediatric Diabetes
|
March 21, 2017
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotonia
S E Flanagan, F Vairo, M B Johnson, et al.
Page
of 59
Search research articles
Search
Showing results (271-280 of 582) with videos related to
Sort By:
Page
of 59
Diabetes
|
May 30, 2006
HLA genotyping supports a nonautoimmune etiology in patients diagnosed with diabetes under the age of 6 months
Emma L Edghill, Rachel J Dix, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 29, 2020
Heterozygous Insulin Receptor <i>(INSR)</i> Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series
Aashish Sethi, Nicola Foulds, Sarah Ehtisham, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
January 8, 2015
Complex equilibria, speciation, and heteroprotein coacervation of lactoferrin and β-lactoglobulin
Sean E Flanagan, Alexander J Malanowski, Ebru Kizilay, et al.
BMC Health Services Research
|
July 19, 2023
Rapid implementation of Veterans Health Administration telehealth creative arts therapies: survey evaluation of adoption and adaptation
Kristin M Story, Mindy E Flanagan, Sheri L Robb, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
January 18, 2003
The influence of insulin on circulating ghrelin
Daniel E Flanagan, Mark L Evans, Teresa P Monsod, et al.
Journal of the American Academy of Dermatology
|
January 9, 2022
Use of virtual reality during scalp injections: A randomized interventional crossover study
James T Pathoulas, Kelly E Flanagan, Chloe J Walker, et al.
Pediatric Diabetes
|
June 4, 2021
Identification of GCK-maturity-onset diabetes of the young in cases of neonatal hyperglycemia: A case series and review of clinical features
Alice E Hughes, Elisa De Franco, Evgenia Globa, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 20, 2014
Congenital hyperinsulinism in a newborn with a novel homozygous mutation (p.Q392H) in the ABCC8 gene
Deniz Anuk Ince, Nursel Muratoglu Sahin, Ayse Ecevit, et al.
JDR Clinical and Translational Research
|
December 1, 2025
Indigenous Australians' Oral Health Care Experiences: Recommendations for Culturally Safe Dental Care
R Aiyar, S Nath, J Hedges, et al.
Pediatric Diabetes
|
March 21, 2017
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotonia
S E Flanagan, F Vairo, M B Johnson, et al.
Page
of 59